A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16901154



Internal ID1581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24017085..24023271hg38UCSC Ensembl
chr1:24343575..24349761hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg386187
hg196187
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422197
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16901154
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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